Results 21 to 30 of about 38,082 (231)

Catalysed oxidation of quinoline in model fuel and the selective extraction of quinoline-N-oxide with imidazoline-based ionic liquids

Egyptian Journal of Petroleum, 2018
Synthesised vanadium-coordinated N,N-bis(o-hydroxybenzaldehyde)phenylene diamine catalyst, [VO(sal-HBPD)] and supported catalyst, p[VO(sal-HBPD)] were employed for the oxidation of quinoline.
Adeniyi S. Ogunlaja, Olalekan S. Alade
doaj   +1 more source

Synthesis and biological evaluation of novel quinoline analogs of ketoprofen as multidrug resistance protein 2 (MRP2) inhibitors [PDF]

Iranian Journal of Basic Medical Sciences, 2021
Objective(s): A new series of quinoline analogs of ketoprofen was designed and synthesized as multidrug resistance protein 2 (MRP2) inhibitors using ketoprofen as the lead compounds.Materials and Methods:  The cytotoxic activity of the compounds was ...
Fatemeh Mosafa, Farzin Hadizadeh, Faezeh Fathi, Zahra Eslami Nasab, Tahereh Pourzahed, Sayyed Mohammad Aboutorabzade, Razieh Ghodsi   +6 more
doaj   +1 more source

PERHALIDES OF QUINOLINE. [PDF]

Journal of the American Chemical Society, 1899
n ...
openaire   +2 more sources

Ag─S Sites Steer Furfural Electroreduction to Furfuryl Alcohol

Angewandte Chemie, EarlyView.
A simple sulfide incorporation strategy turns silver into a highly active and selective catalyst for furfural electroreduction to furfuryl alcohol. Experiments combined with density functional theory reveal how isolated S sites promote hydrogenation while suppressing hydrofuroin coupling, enabling selective biomass upgrading.
Haibin Ma, Jordi Morales‐Vidal, George Teo, Muhammad S. Naeem, Terence Jing Cong Tan, Núria López, Boon Siang Yeo   +6 more
wiley   +2 more sources

1‐Azabicyclo[1.1.0]butanes (ABBs) on the Map: Mechanistic Pathways for Catalytic Ring Opening and Functionalizations

Angewandte Chemie, EarlyView.
Catalytic strain‐release ring opening and functionalizations of 1‐azabicyclo[1.1.0]butanes (ABBs) represent a promising strategy for accessing diverse azetidine products. These transformations proceed via polar pathways, radical pathways, and hybrid mechanisms that combine both.
James Shao‐Jiun Yang, Hsuan‐Hung Liao   +1 more
wiley   +2 more sources

2-(2,4-Dichlorophenyl)-9-phenyl-2,3-dihydrothieno[3,2-b]quinoline

Acta Crystallographica Section E, 2009
In the title compound, C23H15Cl2NS, the quinoline system is almost planar [r.m.s. deviation = 0.013 (2) Å]. The phenyl group is disordered over two positions with site occupancies of 0.55 and 0.45, and is oriented in a nearly
K. Balamurugan, D. Narmadha, J. Suresh, S. Perumal, P. L. Nilantha Lakshman   +4 more
doaj   +1 more source

Effective degradation of quinoline by catalytic ozonation with MnCexOy catalysts: performance and mechanism

Water Science and Technology
Quinoline inevitably remains in the effluent of coking wastewater treatment plants due to its bio-refractory nature, which might cause unfavorable effects on human and ecological environments.
Jie Zhang, Zhaochang Wu, Ben Dong, Sijie Ge, Shilong He   +4 more
doaj   +1 more source

A role for eIF5A in translational control of stress‐inducible proteins in multiple myeloma cell lines

Molecular Oncology, EarlyView.
Loss of eIF5A rewires thapsigargin‐mediated endoplasmic reticulum stress responses in multiple myeloma cells by selective translation of mRNA transcripts, consequently dampening thapsigargin‐induced unfolded protein response (UPR) activation and shifting the balance from induction of apoptosis toward cell survival and proliferation.
Demi Both, Ingrid A. M. Derks, Raphaël Vanleyssem, Marine Leclercq, Najla El Hachem, Pierre Close, Eric Eldering, Marco Vincent Haselager   +7 more
wiley   +1 more source

Ligand‐Directed Molecular Beacons as Turn‐On Fluorescent Probes for Sensing Cell‐Surface Receptor‐Ligand Interactions

Angewandte Chemie, EarlyView.
Multivalent, ligand‐directed molecular beacons enable fluorescence turn‐on detection of cell‐surface receptors in living cells. The probes strongly engage closely spaced membrane receptors and exhibit conformation‐dependent fluorescence enhancement at the cell surface, enabling wash‐free receptor imaging, inhibitor screening, and functional evaluation ...
Noa Oppenheimer‐Low, Denis Shpalter, Suraj Toraskar, Martín López‐Vidal, Ziv Porat, Inna Goliand, Ekaterina Petrovich‐Kopitman, Noga Kozer, Haim Michael Barr, Alla H. Falkovich, Leila Motiei, David Margulies   +11 more
wiley   +2 more sources

Synthesis, Electrochemical and Spectroscopic Characterization of Selected Quinolinecarbaldehydes and Their Schiff Base Derivatives

Molecules, 2020
A new approach to the synthesis of selected quinolinecarbaldehydes with carbonyl groups located at C5 and/or in C7 positions is presented in this paper in conjunction with spectroscopic characterization of the products.
Jakub Wantulok, Marcin Szala, Andrea Quinto, Jacek E. Nycz, Stefania Giannarelli, Romana Sokolová, Maria Książek, Joachim Kusz   +7 more
doaj   +1 more source